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@Jo_Perpetual 

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Jo_Perpetual

I

I was diagnosed about 9 months ago. I recently started coming to terms with my diagnosis, though most times i try to ignore it, it somehow stick its head in my business.

@Chris_Patrie 

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Chris_Patrie

New to Aubagio

started one month ago and having some stomach/digestive issues. Posted list of side effects says this should pass in two weeks. Not my experience and asking others if they’ve experienced anything similar. thanks

@Bob2393 

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Bob2393

Shoes

Hello, was diagnosed in March after two surgeries. I’m learning everyday of what my body can do and cannot. Each day a lil different. My one leg does not follow”directions “ and quite often “drags” . Wondering if any body can suggest a brand or o line of shoes, that might help. Thank you

@Indie 

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Indie

Mavenclad and instruction to Shield

<p>Hi 👋 I completed my first round of Mavenclad in February of this year and received my letter from the Government asking me to “Shield” for 12 weeks in March, due to the risk of possible complications from COVID-19. At that time my lymphocytes were 0.8. Does anyone know what lymphocyte level we a...</p>

@Jill0827 

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Jill0827

High humidity cooler temps

Some of my worst symptoms come during high humidity- regardless if temps are hotter or cooler. It’s a “heavy” feeling in my head that is difficult to describe (not a headache) but leads to nausea, dizziness and overall misery. I see my neuro on Monday so will ask her but I can’t seem to find ways to...

@Bobbij 

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Bobbij

Spinal tap

I'm going for a spinal tap in 6 weeks or so, been doing some reading about the procedure and after care, what has been anyone's experience after having one done. Seems to be alot of complain g of back pain and headache

@Karen_Sue_Thacker 

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Karen_Sue_Thacker

Early signs and symptoms of MS

Can someone please elaborate what are some of the early signs and symptoms of the disease? How do I approach the subject with my physician?

Just Because

Hello everyone. Just wanted to say I thankful for all the new people I have met so far. I like hearing everyone's personal story, and all the great advice. This is truly an informative place with lovely people. Stay safe friends.

@VanBax 

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VanBax

Amantadine

Hi all. Does anyone have any experiences of taking Amantadine for MS fatigue. I am currently taking modafinil x 2 100g first thing each day but still suffer from chronic fatigue in the afternoons. MS Nurse has recommended switching to Amantadine. I’m happy to switch but reluctant to give up moda...

@Bobbij 

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Bobbij

Benign MS

I was just diagnosed with benign MS not quite sure about it as of yet, all I know is my symptoms with Tingling in the scalp, right arm, pain in those areas also plus right leg, are very real, but I guess will know more once I get to see the MS specialist